Product Details

SNP ID
rs4958531
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:152392277 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTGCTGGGAGGTGAGAGTTGTGCA[C/T]GGATGACTGACATGGGAATTGGGGA
Phenotype
MIM: 605108
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NMUR2 PubMed Links

Gene Details

Gene
NMUR2
Gene Name
neuromedin U receptor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020167.4 1328 Missense Mutation ATG,GTG M388V NP_064552.3
XM_011537670.2 1328 Intron XP_011535972.1

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